- Open Access
Transcriptome profile analysis reflects rat liver and kidney damage following chronic ultra-low dose Roundup exposure
© Mesnage et al. 2015
Received: 21 April 2015
Accepted: 11 August 2015
Published: 25 August 2015
The Erratum to this article has been published in Environmental Health 2017 16:28
Glyphosate-based herbicides (GBH) are the major pesticides used worldwide. Converging evidence suggests that GBH, such as Roundup, pose a particular health risk to liver and kidneys although low environmentally relevant doses have not been examined. To address this issue, a 2-year study in rats administering 0.1 ppb Roundup (50 ng/L glyphosate equivalent) via drinking water (giving a daily intake of 4 ng/kg bw/day of glyphosate) was conducted. A marked increased incidence of anatomorphological and blood/urine biochemical changes was indicative of liver and kidney structure and functional pathology. In order to confirm these findings we have conducted a transcriptome microarray analysis of the liver and kidneys from these same animals.
The expression of 4224 and 4447 transcript clusters (a group of probes corresponding to a known or putative gene) were found to be altered respectively in liver and kidney (p < 0.01, q < 0.08). Changes in gene expression varied from −3.5 to 3.7 fold in liver and from −4.3 to 5.3 in kidneys. Among the 1319 transcript clusters whose expression was altered in both tissues, ontological enrichment in 3 functional categories among 868 genes were found. First, genes involved in mRNA splicing and small nucleolar RNA were mostly upregulated, suggesting disruption of normal spliceosome activity. Electron microscopic analysis of hepatocytes confirmed nucleolar structural disruption. Second, genes controlling chromatin structure (especially histone-lysine N-methyltransferases) were mostly upregulated. Third, genes related to respiratory chain complex I and the tricarboxylic acid cycle were mostly downregulated. Pathway analysis suggests a modulation of the mTOR and phosphatidylinositol signalling pathways. Gene disturbances associated with the chronic administration of ultra-low dose Roundup reflect a liver and kidney lipotoxic condition and increased cellular growth that may be linked with regeneration in response to toxic effects causing damage to tissues. Observed alterations in gene expression were consistent with fibrosis, necrosis, phospholipidosis, mitochondrial membrane dysfunction and ischemia, which correlate with and thus confirm observations of pathology made at an anatomical, histological and biochemical level.
Our results suggest that chronic exposure to a GBH in an established laboratory animal toxicity model system at an ultra-low, environmental dose can result in liver and kidney damage with potential significant health implications for animal and human populations.
Glyphosate-based herbicides (GBH), such as Roundup, are the major pesticides used worldwide. GBH are currently applied on at least 24 % of the total global cropland (Benbrook C, personal communication), and also used extensively in domestic and urban environments. Residues of GBH are routinely detected in foodstuffs [1, 2] and also drinking water contaminated via rain, surface runoff and leaching into groundwater, thereby increasing possible routes of exposure . Epidemiological data on the human body burden of GBH residues is very limited but evidence suggests that glyphosate and its metabolites are wide-spread .
Glyphosate’s primary perceived mode of herbicidal action is to inhibit 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) of the shikimate aromatic amino acid biosynthesis pathway present in plants and some bacteria. Since this pathway is absent in vertebrates, it is generally assumed that glyphosate poses minimal health risks to mammals, including humans . However, converging evidence suggests that GBH residues pose a particular risk to kidney and liver function. Hepatic effects of glyphosate were first observed in the 1980s, including its ability to disrupt liver mitochondrial oxidative phosphorylation . As glyphosate can act as a protonophore increasing mitochondrial membrane permeability to protons and Ca2+ , it can trigger the production of reactive oxygen species resulting in observed oxidative stress . Elevation in oxidative stress markers is detected in rat liver and kidney after subchronic exposure to GBH at the United States permitted glyphosate concentration of 700 μg/L in drinking water . Hepatic histological changes and alterations of clinical biochemistry are detected in rats consuming 4.87 mg/kg body weight (bw) glyphosate every 2 days over 75 days .
Metabolic studies in a variety of laboratory and farm animals show levels of glyphosate and aminomethylphosphonic acid (AMPA, the principal breakdown product of glyphosate) in kidney and liver tissues that are 10- to 100-fold or even greater than the levels found in fat, muscle, and most other tissues . In farm animals, elevated glyphosate urinary levels are correlated with alterations in blood serum parameters indicative of liver and kidney oxidative stress and depletion in nutrient trace element levels .
In addition to these cytotoxic effects, studies have suggested that GBH can disrupt several endocrine-signaling systems, including estrogen  and retinoic acid . Endocrine disruptive effects may explain reproductive developmental impairment in rats exposed to sub-lethal doses of GBH . Effects on retinoic acid signalling pathways have been proposed to account for the potential teratogenic effects of GBH in mammals  and amphibians .
Nevertheless, it should be noted that most results from these GBH toxicity studies were obtained at doses far greater than general human population exposure. Doses tested were typically over the glyphosate acceptable daily intake (ADI), which is currently set at 0.3 mg/kg bw/day within the European Union and 1.75 mg/kg bw/day in the USA based on hepatorenal toxicity measurements after chronic exposure in rats, although GBH toxicity was not investigated in life-long experiments.
In order to address this issue, a 2-year study was conducted where rats were administered via drinking water at a concentration of 0.1 ppb Roundup, thus containing not only glyphosate but also adjuvants . The glyphosate equivalent concentration was 0.05 μg/L and corresponds to an admissible concentration within the European Union (0.1 μg/L) and USA (700 μg/L). The results showed that Roundup caused an increased incidence of anatomical signs of pathologies, as well as changes in urine and blood biochemical parameters suggestive of liver and kidney functional insufficiency in both sexes. In an effort to confirm these findings through a more quantitative molecular biological approach and obtain insight into the alterations in gene expression profiles associated with the observed increased signs of kidney and liver anatomorphological pathologies, we conducted a full transcriptomic analysis of these organs from the female cohort of animals. A large number of transcript clusters (>4000) were found to be altered in their level of expression in both the liver and kidneys of the Roundup treated group relative to controls and to a very high statistical significance. The alterations in gene expression profiles are typical of disturbances measured in cases of fibrosis, necrosis, phospholipidosis, mitochondrial membrane dysfunction and ischemia. Therefore our results confirm the ultra-low dose Roundup-induced increased incidence of hepatorenal pathologies suggested by observations at an anatomical, histological and biochemical level.
The tissues analyzed in this study were obtained from animals as previously described . Briefly, the experimental protocol was as follows. Following 20 days of acclimatization, 5 week old Harlan Sprague–Dawley rats were randomly assigned on a weight basis into groups of 10 animals. Animals were fed with the standard diet A04 (Safe, France) including 33 % maize DKC 2675 over 2 years. All feed formulations consisted of a balanced diet, chemically measured as substantially equivalent. All animals were kept in polycarbonate cages (820 cm2, Genestil, France). The location of each cage within the experimental room was regularly changed. The litter (Toplit classic, Safe, France) was replaced twice weekly. The animals were maintained at 22 ± 3 °C under controlled humidity (45 to 65 %) and air purity with a 12 h-light/dark cycle, with free access to food and water. All reagents used were of analytical grade. The animal experimental protocol was conducted in accordance with the regulations of the local ethics committee in an animal care unit authorized by the French Ministries of Agriculture and Research (Agreement Number A35-288-1). Animal experiments were performed according to ethical guidelines of animal experimentation (regulation CEE 86/609).
Groups of 10 animals had access to either plain water (control) or to the same water supplemented with 1.1e-8 % of Roundup (0.1 ppb or 50 ng/L glyphosate equivalent dilution). The commercial formulation of Roundup used was Grand Travaux Plus (450 g/L glyphosate, approval 2020448; Monsanto, Belgium). The required level of Roundup dilution in drinking water was confirmed by measurement of glyphosate concentration by HPLC-MS/MS. Similarly, glyphosate stability in solution was studied and validated during the 7 day period between two preparations of the test, treatment solutions. Glyphosate and AMPA were not found in the feed at the limit of detection of 5 mg/kg.
Twice-weekly monitoring allowed careful observation and palpation of animals, recording of clinical signs, identification and measurement of any tumours, food and water consumption, and individual body weight. Measurement of mortality rates, anatomopathology (on 34 different organs), serum biochemistry (31 parameters) and urine composition (11 parameters) have been extensively described .
For transmission electron microscopy, liver fragments were fixed in pre-chilled 2 % paraformaldehyde/2.5 % glutaraldehyde in 0.1 M phosphate buffered saline pH 7.4 at 4 °C for 3 h and processed as previously described . Evaluation of cell, cytoplasm and nuclear area, and nuclear-cytoplasmic ratio was determined from measurements on 30 hepatocytes per animal. Cell nuclear parameters (% heterochromatin, pore density, fibrillar centers area, % fibrillar centers, % dense fibrillar components and % granular components) were measured on 10 nuclei per animal.
Tissue sampling and RNA extraction
Animals were sacrificed at the same time of day during the course of the study either to comply with animal welfare regulations to avoid unnecessary suffering (for example, resulting from 25 % body weight loss, presence of tumours over 25 % bodyweight, hemorrhagic bleeding, or prostration) or at the termination of the study period of 2 years. Animals were sacrificed by exsanguination under isoflurane anesthesia. The liver was divided into two portions; one was snap frozen in liquid nitrogen/dry ice and stored at −80 °C. One kidney was also snap frozen. (Note: due to handling errors at the company employed to conduct the experiment, one kidney sample from the Roundup treatment group was unavailable for analysis).
Transverse cross sectional slices of liver and kidneys were processed for total RNA extraction using MagMax-96 for Microarrays Total RNA Isolation Kit (Ambion, Life Technologies Ltd, Paisley, UK).
Total RNA (500 ng) was labelled using terminal deoxynucleotidyl transferase (TdT) in the presence of a proprietary biotinylated compound using the Ambion whole transcript Expression kit and the whole transcript Terminal Labelling kit (Affymetrix UK Ltd., High Wycombe, UK), following standard protocols. We employed the Affymetrix GeneChip® Rat Gene 2.0 ST Array containing approximately 610,400 probes grouped into 214,300 exon-level and 26,400 gene-level probe sets. The median number of probes per transcript is 22, usually distributed along the entire transcript sequence. Overall, this microarray covers 28,407 refseq transcripts including 16,771 protein coding transcripts. By comparison, version 5.0 annotation of the rat (strain BN/SsNHsdMCW) genome assembly contains 30,404 transcripts including 22,777 coding genes. The analysis was performed at the level of transcript clusters. We also used the MetaCore Analytical Suite to perform the transcription factor and the pathway and toxicity process analysis based on network objects recognized by MetaCore.
Hybridisation cocktails were applied to Affymetrix Rat Gene 2.0 microarrays, and processed in accordance with the manufacturer’s recommended procedure using the GCS3000 microarray system (Affymetrix). Array data was exported as cell intensity (CEL) files for further analysis.
Microarray data analysis
CEL files were normalised together in the Expression Console software package (Affymetrix), using the Robust Multi-array Average (RMA) sketch algorithm (gene-level). Data was quality control assessed by using standard metrics and guidelines for the Affymetrix microarray system. Normalised data files (CHP files) were imported into Omics Explorer 3.0 (Qlucore) for further quality control and statistical analysis. It was decided to include all genes in the tests as there is no simple measure of presence/absence with RMA normalized data from Rat Gene 2.0 ST arrays. Although it risks a higher false discovery rate, all data collected were subjected to the statistical tests so as not to inadvertently filter out important genes based on an arbitrary detection threshold. Data used for the functional analysis were selected at the cut off values of p < 0.01 with FC >1.1 to use large gene lists as recommended . The q-values, an estimate of the false discovery rate, were the p-values corrected using the Benjamini-Hochberg procedure and were below 8 %.
Gene ontology, pathways, gene networks, transcription factor binding and disease ontology were analyzed using the Thomson Reuters MetaCore Analytical Suite recognizing network objects (proteins, protein complexes or groups, peptides, RNA species, compounds among others) and/or the NIH Database for Annotation, Visualization and Integrated Discovery Bioinformatics Resources 6.7, recognizing individual coding genes, using recommended analytical parameters . These microarray data have been submitted to Gene Omnibus and are accessible through accession number GSE66060.
Microarray data validation by real-time qPCR
In order to validate the list of differentially expressed/regulated genes revealed by microarray analysis, we randomly selected a subset of 18 genes for analysis by real-time quantitative PCR (RT-qPCR) using the original RNA samples as starting material. Total RNA (2 μg) was converted to cDNA with the High Capacity RNA-to-cDNA kit (Applied Biosystems, Life Technologies Ltd, Paisley, UK), and gene expression measurements were assessed by RT-qPCR using TaqMan Gene Expression assays and TaqMan Universal PCR Master Mix (Applied Biosystems). Housekeeping genes used as endogenous controls were of two types: 1) three standard historically used housekeeping genes (Gapdh, Hprt1, Actb) (from the GeNorm list) as being among the most invariant transcript clusters from microarray datasets; that is, genes with the lowest standard deviation across all relevant samples, and with high or comparable expression level, and 2) Pes1, a gene which is not sex- and/or multi-hormone-regulated in rat studies . Delta Ct methods were used to normalise the expression of the chosen genes of interest against the average of the endogenous control genes. Group fold changes and log ratios (relative to control groups) were calculated using the RQ method in DataAssist v3.0 software (Applied Biosystems).
The rat liver and kidney tissues that formed the starting material for this investigation were obtained from animals that formed part of a chronic (2 year) toxicity study looking at the effects of Roundup pesticide . Roundup was administered via drinking water to Sprague–Dawley rats at a regulatory admissible dose (50 ng/L glyphosate equivalent dilution) and which is representative of what may be found in contaminated tap water. At this dose, the glyphosate equivalent average daily intake of Roundup was approximately 4 ng/kg bw/day of glyphosate.
Male animals suffered from liver and kidney damage more acutely than females, resulting in an increased rate of premature death . Most male rats were discovered after death had occurred. This resulted in organ necrosis making them unsuitable for further analysis and thus they were excluded from transcriptome profiling. We therefore focused our investigation on female animals where freshly dissected tissues from cohorts of 9–10 euthanised treated and untreated rats were available.
Female control and Roundup-treated animals were respectively euthanized at 701 +/− 62 and 635 +/− 131 days (Additional file 1). Anatomopathological analysis of organs from these animals revealed that the liver and kidneys were the most affected organs . Roundup-treated female rats showed 3 times more anatomical signs of pathology (15 in 8 rats) than the control group (6 in 4 rats). In addition, serum and urine biochemical analysis showed increased levels of serum triglycerides. While no severe anatomical kidney damage was detected, biochemical analysis revealed a decrease in blood Na, Cl, P and K levels and a corresponding increase in urine suggesting ion leakage and decreased urinary creatinine. Taken together these alterations in blood and urinary biochemical parameters suggest an impairment of kidney function. Overall, twice the number of biochemical parameters was disturbed in kidney than what can be expected by chance. Furthermore, a testosterone/estrogen imbalance was evident with testosterone serum levels significantly increased by 97 % by comparison to controls, while estradiol serum levels were decreased by 26 %. These observations together with pituitary gland disturbances suggest endocrine disrupting effects.
Transcriptome patterns segregate liver and kidney samples based on Roundup treatment
Number of transcript clusters whose expression is disturbed at different cut-off threshold p-values
Out of these, 18 genes were randomly selected for validation of the microarray results by RT-qPCR (Additional file 6). The overall pattern of the RT-qPCR results confirmed the microarray data with 86 % of the genes found to be similarly up- or down-regulated by both methods.
Gene function alterations involved in mitochondrial respiration, spliceosome function and chromatin structure modification is associated with Roundup treatment
Functional clustering of genes derived using the DAVID gene functional classification tool
Term in DAVID
GO:0010558 ~ negative regulation of macromolecule biosynthetic process
GO:0031327 ~ negative regulation of cellular biosynthetic process
GO:0009890 ~ negative regulation of biosynthetic process
GO:0016279 ~ protein-lysine N-methyltransferase activity
GO:0016278 ~ lysine N-methyltransferase activity
GO:0018024 ~ histone-lysine N-methyltransferase activity
GO:0042054 ~ histone methyltransferase activity
GO:0008276 ~ protein methyltransferase activity
GO:0000377 ~ RNA splicing, via transesterification reactions with bulged adenosine as nucleophile
GO:0000375 ~ RNA splicing, via transesterification reactions
GO:0000398 ~ nuclear mRNA splicing, via spliceosome
IPR000504:RNA recognition motif, RNP-1
IPR012677:Nucleotide-binding, alpha-beta plait
GO:0006099 ~ tricarboxylic acid cycle
GO:0046356 ~ acetyl-CoA catabolic process
GO:0009109 ~ coenzyme catabolic process
GO:0009060 ~ aerobic respiration
GO:0051187 ~ cofactor catabolic process
rno00020:Citrate cycle (TCA cycle)
GO:0006084 ~ acetyl-CoA metabolic process
GO:0030964 ~ NADH dehydrogenase complex
GO:0045271 ~ respiratory chain complex I
GO:0005747 ~ mitochondrial respiratory chain complex I
GO:0005746 ~ mitochondrial respiratory chain
GO:0016571 ~ histone methylation
GO:0008213 ~ protein amino acid alkylation
GO:0006479 ~ protein amino acid methylation
First, two clusters were related to spliceosome function. This included genes encoding cleavage and polyadenylation specific factors (Cpsf2, Cpsf3 and Cpsf7), heterogeneous nuclear ribonucleoproteins (Hnrnpl, Hnrnpf) and splicing factors (Sf3b5, Sf3a1). Expression of all of these genes was upregulated with the exception of Cpsf3. Other genes involved in RNA splicing, such as Luc7l3, Pnn, Prpf4b, Pnisr, Prpf39, Srek1, Ddx39b and Ddx39a, were significantly upregulated. Additionally, expression of at least 160 non-coding snoRNAs were found to be altered with almost all being upregulated with a large FC of up to 5.32 for ENSRNOT00000068958in kidneys. Second, two clusters consisted of members of the chromatin modification family of enzymes, in particular histone-lysine N-methyltransferases. Expression of the 7 genes (Men1, Setdb1, Suv420h2, Dot1l, Ehmt1, Ehmt2, Nsd1) belonging to this cluster was upregulated. Other genes with a related ontology (Mll2, Mll4, Tet3, Baz2a, Dnmt3a, Brd1, Brd4, Ino80d or Arid4b), which are not taken into account in the cluster of enriched biological functions, were also upregulated. Most also belong to the family of histone-lysine N-methyltransferase complexes that specifically methylate lysine residues of histone H3 (Lys-4, 9, 20 or 79) or H4 (Lys-20) among others, tagging them for chromatin condensation. In addition, most of these are also included in a larger disturbed cluster of 40 genes involved in negative regulation of macromolecule biosynthetic processes.
Third, functional disturbance of genes involved in mitochondrial metabolism was represented by two clusters, especially related to respiratory chain complex I and the TCA cycle. Expression of most of these genes was repressed. A total of 7 genes encoding NADH dehydrogenase (ubiquinone) complex I of the mitochondrial respiratory chain were found disturbed, with 6 of them being downregulated. Additionally, the genes encoding isocitrate dehydrogenases (Idh3B and Idh3g), succinate dehydrogenase (Sdhc), succinate-CoA ligases (Sucla2 and Suclg2) and mitochondrial F1 complex ATP synthases (Atp5b and Atp5d) were downregulated. These data suggest that activities of mitochondrial complexes, in particular respiratory activity, are depressed.
Roundup-associated changes may occur via sex-hormone signaling pathways
The gene ontology analysis (Table 2) indicates a modulation of cell signalling pathways has taken place. The GO biological processes GO:0007264 “small GTPase mediated signal transduction” (21 genes, p = 1.2E-3, q = 1.2E-1) and GO:0007242 “intracellular signalling cascade” (57 genes, p = 2.2E-3, q = 1.7E-1) are enriched among genes commonly disturbed in liver and kidneys. Additionally, the networks highlighted by this analysis that may account for the disturbance in gene expression were centred on the transcription factors Creb1 (280 genes regulated, p ~ 0), c-Myc (159 genes regulated, p ~ 0), Yy1 (113 genes regulated, p <4.8E-234), Oct3/4 (94 genes regulated p <6.7E-194) and Esr1 (83 genes regulated, p <8.E-171) (Additional file 7). These transcription factors are intimately connected in regulation of gene expression and can be involved in hormone signalling pathways.
In this context, it is noteworthy that the gene encoding the androgen receptor is statistically significantly downregulated in liver (FC = −1.4, p = 8.1E-3, q = 7.7E-2) and kidneys (FC = −1.32, p = 2.9E-3, q = 3.8E-2). In addition, the retinoid X receptor beta gene (Rxrb) is significantly upregulated in liver (FC = 1.2, p = 3.5E-5, q = 3.2E-3) and kidneys (FC = 1.36, q = 4.5E-6, q = 1.2E-3). In addition, the KEGG annotation for the mTOR signalling pathway (14 genes, p = 6.4E-3, q = 0.21) and the phosphatidylinositol signalling system (16 genes, p = 1.3E-2, q = 0.29) are enriched in liver. In kidney, the KEGG annotation for the adipocytokine signalling pathway (involving mTOR) (19 genes, p = 2.4E-3, q = 0.06) and the phosphatidylinositol signalling system (21 genes, p = 6E-4, q = 0.05) are enriched. However, expression of Star, which has been suggested by previous studies to mediate endocrine disrupting effects of Roundup in MA-10 Leydig tumor cells , and of Esr1, Esr2 and aromatase (Cyp19a1), which were found disturbed in the human HepG2 hepatocyte cell line , were not found to be dysregulated in this investigation.
Alterations in transcriptome profile suggest liver and kidney anatomorphopathogy
Furthermore, the GO “metabolic process” and “cellular response to stress” processes have low p-values in liver (respectively p = 3.7E-58 and 3.9E-16) and kidneys (p = 1.5E-49 and 1.0E-14), which strongly suggest a state of metabolic stress. Overall, toxicity process analysis revealed gene expression disturbances associated with apoptosis, necrosis, phospholipidosis, mitochondrial membrane dysfunction and ischemia. Thus the alteration in the transcriptome profile identified in this study correlates with the observed increased signs of anatomical and functional pathology of the liver and kidneys.
We report here the first in vivo transcriptome investigation in a mammalian species following long-term (2 year) exposure to an agricultural GBH (Roundup) at an environmentally relevant dose. Our results confirm the increased incidence of liver and kidney pathologies described at an anatomorphological and blood/urine biochemical level in female rats administered with Roundup in drinking water at a regulatory admissible, ultra-low dose 50 ng/L glyphosate equivalent concentration . The levels of glyphosate consumption were approximately 4 ng/kg bw/day, which are well below global ADI values. We observed a wide-scale, treatment-associated alteration in gene expression patterns at a high statistical significance in both the liver and kidneys (Figs. 2 and 3; Table 1). Gene ontology analysis of these transcriptome alterations is linked with a marked change in mitochondrial respiration, spliceosome activity, chromatin structure and hormone signalling pathways (Table 2). Collectively, the alterations in gene expression (Fig. 4) are associated with a deregulation of tissue homeostasis at the level of proliferation-apoptosis balance (Fig. 5) and thus correlates well with the increased signs of liver and kidney anatomical, histological and blood/urine biochemical pathologies described in these animals . Also of note is that the Roundup-treatment associated alterations in gene expression patterns we observe do not correspond to transcriptome signatures of liver necrosis provoked by acute hepatotoxicants .
Following the recommended analytical approach for large sets of genes , we observed a large number (>4000) whose expression was altered in both the liver and kidneys within the Roundup treatment group (Fig. 3a). In the majority of cases the change in level of transcription was below 2-fold (Fig. 3a and b) but to a highly statistically significant degree (p <0.01). These observations imply that low but consistent changes in expression of a large number of genes can provide sufficient statistical resolution to be informative regarding any organ pathology that may be present.
However, given the large number of gene functions altered in both the liver and kidneys within the Roundup treatment group, this represents a combination of effects resulting from the pathology of these organs as well as a direct impact of the pesticide. Thus it is not possible from our investigation to definitively distinguish the primary effects of Roundup on the liver and kidney transcriptome from the secondary effects on gene expression arising from the pathology present in these organs. Nevertheless, the smaller cohort of genes found to be commonly disturbed in liver and kidney (Fig. 3; Additional file 5) may provide insight into those systems that may be the primary targets of this herbicide (Table 2). Our results highlight the need for future GBH toxicity studies where organ transcriptome is determined prior to appearance of the overt liver and kidney pathologies observed at late-stage termination as in this instance. Thus transcriptome disturbances that may ultimately lead to the later stage organ pathologies may be identified. In addition, the clinical relevance of our observations remains to be ascertained, particularly as there is limited data available on glyphosate levels within humans .
Findings from studies where mice were fed diets containing Roundup-tolerant genetically modified soybeans [18, 24] are consistent with our observations. Animals showed disruptions in hepatocyte nuclear architecture, decreased expression of certain respiratory enzymes, a disturbance of splicing activity and marked increased liver ageing. In addition, similar observations were made with rat hepatocytes treated with Roundup in vitro , suggesting that alterations in nucleolar and mitochondrial function may be a direct primary effect of this herbicide.
Previous studies, albeit at much higher doses, have shown that glyphosate can uncouple liver mitochondrial oxidative phosphorylation  and induce non-specific membrane permeabilization and a depletion of succinate-dependent respiratory indexes in isolated rat mitochondria . The mode of glyphosate inhibition of EPSPS in plants is by competitive inhibition of phosphoenolpyruvate (PEP) substrate binding at the enzyme active site . Enzymes binding PEP are regulators of energy metabolism in particular through the TCA cycle. Glyphosate off-target effects may include the disruption of these enzymes. Indeed, glyphosate can interact at the substrate binding site and potentially inhibit mitochondrial succinate dehydrogenase . Furthermore, as small molecule chelators of zinc can perturb spliceosome assembly and activity of chromatin modifying enzymes , glyphosate may also have exerted direct effects on spliceosome function due to its metal chelating properties (Patent No: US 3160632; ).
The increased incidence of Roundup-associated liver and kidney pathologies  confirmed in this report may be arising from multiple sources as there is increasing evidence to suggest that GBH and glyphosate can bring about toxic effects via different mechanisms depending upon the level of exposure. However, toxic effects have been recorded in most instances at levels of glyphosate and/or GBH exposures [10, 15] far in excess of the ultra-low dose administered to the animals in this investigation. Thus it is difficult to definitively attribute one or more mechanisms of toxicity observed at these higher dose levels to the liver and kidney pathologies seen in our study. Nevertheless, our observation of a major accumulation of snoRNAs in both liver and kidneys of the Roundup-treated group (Fig. 3, Table 2) supports the possibility of damage arising from oxidative stress as these are known to play a critical role in amplifying the effects of reactive oxygen species and downstream oxidative stress-mediated tissue injury . The study by Michel and colleagues demonstrated the induction of snoRNA expression as a functional link between the progress of lipotoxic cell death and the deleterious cellular response to oxidative stress . Lipotoxicity manifests itself as enhanced oxidative stress and as elevated proinflammatory signalling, often associated with abnormal insulin action . It is noteworthy that we found disturbances in the pathways associated with these biological processes in our study (Fig. 5).
In addition, the analysis of pathways revealed disturbances in the modulation of mTOR and phosphatidylinositol signalling systems, both linked to the regulation of lipid synthesis among other major cellular functions . Phosphoinositide 3-kinase transduces signals from various factors into intracellular messages by generating phospholipids, the disruption of which is among the major toxicity endpoint processes observed in the liver and kidneys in this study (Fig. 5). Overall, these results suggest an involvement of lipotoxic stress associated with elevated oxidative stress and proinflammatory signalling, which is a hallmark of chronic liver and kidney disease .
Chronic lipotoxic conditions in our study are also corroborated by biochemical analysis showing increased levels of serum triglycerides . In some circumstances, excess free fatty acids induce apoptotic cell death . Our analysis also indicates changes in intracellular pathways possibly underlying a change in cell growth, such as the proinsulin C-peptide signalling pathway as well as the mTOR and the phosphatidylinositol signalling systems. Tissue homeostasis relies on a delicate balance between apoptosis and cellular proliferation. When oxidative stress provokes apoptosis, injured cells are generally replaced through increased proliferation. Interestingly, similar results have recently been reported where transcriptome analysis of brown trout exposed to glyphosate or Roundup at a concentration (10 μg/L) typically found in the environment, revealed an over-representation of pathways involved in oxidative stress, apoptosis, and the regulation of cell proliferation . However, although there is evidence to suggest that glyphosate can inhibit multiple cellular functions such as mitochondrial respiration, and enzyme activities other than EPSPS within the shikimate pathway, the existence of such direct mechanisms of interference at the low environmental dose tested here currently remains unknown and thus needs further exploration.
The proliferation/apoptosis imbalance may also have been either caused or promoted by a chronic disruption of the endocrine system and the activation or repression of signalling pathways. Activation of phosphoinositide 3-kinase (PI3K) by hormones such as estrogens  results in a global downregulation of genes encoding members of the TCA cycle and oxidative phosphorylation, defective mitochondria, and reduced respiration . Hormones and their nuclear receptors have dynamic interactions with chromatin remodeling complexes and spliceosome function . As we have observed a disturbance in estrogen/testosterone balance and pituitary dysfunction in the animals studied here , a link between the disturbed gene expression patterns and pathologies via an endocrine disruptive mechanism is plausible, especially as endocrine disruptive effects can occur at very low doses . Furthermore, the top-scoring transcription factor networks that can account for the observed Roundup-associated alterations in gene expression presented here are centered on Creb1, Esr1, Yy1, c-Myc and Oct3/4 (Fig. 4), which cooperate to regulate gene expression following hormonal stimulation . Hormonal imbalance is generally associated with kidney or liver failure . Furthermore, glyphosate has been found to act as an estrogen agonist in human breast cancer cell assays stimulating growth at comparable concentrations to the native hormone [13, 41]. This estrogenic potential of glyphosate may have contributed to the trend in increased mammary tumor incidence in the Roundup-treated rats analysed in this investigation .
An important consideration is that Roundup is not a single compound, but a mixture of an active ingredient (glyphosate) combined with various adjuvants, which are required to stabilise and allow penetration of glyphosate into plants. In short term acute exposures, some adjuvants can be considered as responsible of Roundup toxicity . However, as adjuvant composition is proprietary and not fully disclosed, it is not possible to attribute the toxicity of the whole agricultural herbicide formulation to a given component. Thus the results from our study are not directly comparable to others testing glyphosate alone. The results we present may be specific for the formulation studied, because the toxicity of different GBH adjuvants can vary by a factor 100 at least based on assays involving a 24 h exposure to human tissue culture cells . Future studies involving the administration of glyphosate alone would shed light on this issue.
In summary, the alterations in transcriptome profile were detected well below the glyphosate ADI (0.3 mg/kg bw/day) set within the European Union, and is within the range admitted in drinking water (0.1 ppb) and foodstuffs (for example, 20 ppm in GM soybeans or 2 ppm in bovine kidneys). As a probable endocrine disruptor, GBH/glyphosate may alter the functioning of hormonal systems and gene expression profiles via different mechanisms depending on the dose. Future metabolomic and proteomic studies of these organs could provide further mechanistic insight into the observed Roundup-mediated pathological process.
It was previously known that glyphosate consumption in water above authorized limits may provoke kidney failure and reproductive difficulties . The results of the study presented here indicate that consumption of far lower levels of a GBH formulation, at admissible glyphosate-equivalent concentrations, are associated with wide-scale alterations of the liver and kidney transcriptome that correlate with the observed signs of hepatic and kidney anatomorphological and biochemical pathological changes in these organs . In addition, as the dose of Roundup we investigated is environmentally relevant in terms of human , domesticated animals  and wildlife [34, 44] levels of exposure, our results potentially have significant health implications for animal and human populations. Furthermore, data also suggests that new studies incorporating testing principles from endocrinology and developmental epigenetics, in particular to evaluate the endocrine disruptive capability of GBH/glyphosate, should be performed to investigate potential consequences of low dose exposure during early life as well as in adults.
This work was funded by the Sustainable Food Alliance (USA), whose support is gratefully acknowledged.
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